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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1642852Generated: October 31, 2026

1-tert-Butoxycarbonylaminocyclopentanecarboxylic acid → Tert-butyl[1-({3-(3-cyclopropyl-1,2,4-oxadiazol-5-yl)-5-[4-(trifluoromethyl)phenyl]piperidin-1-yl}carbonyl)cyclopentyl]carbamate

https://huagongshe.com/reaction/1642852

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-tert-Butoxycarbonylaminocyclopentanecarboxylic acidHCID 2734645—
Reactant3-(3-Cyclopropyl-1,2,4-oxadiazol-5-yl)-5-[4-(trifluoromethyl)phenyl]piperidineHCID 58002519—
ProductTert-butyl[1-({3-(3-cyclopropyl-1,2,4-oxadiazol-5-yl)-5-[4-(trifluoromethyl)phenyl]piperidin-1-yl}carbonyl)cyclopentyl]carbamateHCID 58002603—

Reaction Steps

100 mg (0.30 mmol) of the compound from Example 183A and 75 mg (0.33 mmol) of 1-[(tert-butoxycarbonyl)amino]cyclopentanecarboxylic acid were reacted according to the General Method 7. Yield: 127 mg (78% of theory)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08119663B2
Source datasetuspto-grants-2012_02
ORD IDord-b87f603d83fe459baeef3d668cc2088f
Source noteuspto-grants-2012_02